List of variants in gene TRIO reported as uncertain significance by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_007118.4(TRIO):c.1035T>G (p.Phe345Leu)	rs1736873932
NM_007118.4(TRIO):c.1368G>A (p.Lys456=)
NM_007118.4(TRIO):c.1644G>T (p.Gln548His)	rs1739405858
NM_007118.4(TRIO):c.4535T>C (p.Phe1512Ser)	rs1747843990
NM_007118.4(TRIO):c.5239C>T (p.Pro1747Ser)	rs1053063993
NM_007118.4(TRIO):c.6836-6T>C	rs1364924645

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